Ontology highlight
ABSTRACT:
SUBMITTER: Renata H
PROVIDER: S-EPMC4365795 | biostudies-literature | 2013 Jan
REPOSITORIES: biostudies-literature
Science (New York, N.Y.) 20130101 6115
Here, we report on a scalable route to the polyhydroxylated steroid ouabagenin with an unusual take on the age-old practice of steroid semisynthesis. The incorporation of both redox and stereochemical relays during the design of this synthesis resulted in efficient access to more than 500 milligrams of a key precursor toward ouabagenin-and ultimately ouabagenin itself-and the discovery of innovative methods for carbon-hydrogen (C-H) and carbon-carbon activation and carbon-oxygen bond homolysis. ...[more]